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Items: 1 to 20 of 153

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7062042inversion1nstd229human GRCh38 chr15: 38,786,391-46,534,887 , GRCh37.p13 chr15: 39,078,592-46,827,085 EHD4-AS1, PLA2G4B, 219 more genes
    nsv6973841copy number variation1nstd229human GRCh38 chr15: 41,876,434-43,470,213 , GRCh37.p13 chr15: 42,168,632-43,762,411 CAPN3, STARD9, 43 more genes
    nsv6967689copy number variation1nstd229human GRCh38 chr15: 43,351,993-43,352,159 , GRCh37.p13 chr15: 43,644,191-43,644,357 ADAL
    nsv6967377copy number variation1nstd229human GRCh38 chr15: 43,349,262-43,469,910 , GRCh37.p13 chr15: 43,641,460-43,762,108 ZSCAN29, TP53BP1, 3 more genes
    nsv6966456copy number variation1nstd229human GRCh38 chr15: 43,352,096-43,393,954 , GRCh37.p13 chr15: 43,644,294-43,686,152 ZSCAN29, ADAL, 2 more genes
    nsv6963230copy number variation1nstd229human GRCh38 chr15: 43,278,815-43,334,747 , GRCh37.p13 chr15: 43,571,013-43,626,945 ADAL, LCMT2, 1 more genes
    nsv6959680copy number variation1nstd229human GRCh38 chr15: 43,323,801-43,375,600 , GRCh37.p13 chr15: 43,615,999-43,667,798 ZSCAN29, ADAL, 2 more genes
    nsv6959025copy number variation1nstd229human GRCh38 chr15: 43,354,801-43,360,700 , GRCh37.p13 chr15: 43,646,999-43,652,898 ZSCAN29, ADAL
    nsv6496110copy number variation1nstd223human GRCh38 chr15: 43,175,921-43,650,339 , GRCh37.p13 chr15: 43,468,119-43,942,537 ADAL, EPB42, 19 more genes
    nsv6291560copy number variation1nstd102humanUncertain significance GRCh37 chr15: 43,215,243-44,632,384 , GRCh38.p12 chr15: 42,923,045-44,340,186 PPIP5K1P1-CATSPER2, STRCP1, 44 more genes
    nsv5968271insertion1nstd209human GRCh38 chr15: 43,334,633-43,334,633 , GRCh37.p13 chr15: 43,626,831-43,626,831 ADAL
    nsv5380758copy number variation2nstd102humanUncertain significance GRCh37 chr15: 32,964,879-91,358,519 , GRCh38.p12 chr15: 32,672,678-90,815,289 LOC105370794, HNRNPA1P45, 1173 more genes
    nsv5150529mobile element insertion1nstd203human GRCh38 chr15: 43,347,704-43,347,716 , GRCh37.p13 chr15: 43,639,902-43,639,914 ADAL
    nsv5140984mobile element insertion1nstd203human GRCh38 chr15: 43,334,153-43,334,171 , GRCh37.p13 chr15: 43,626,351-43,626,369 ADAL
    nsv5038422inversion1nstd200human GRCh38 chr15: 40,121,948-64,050,807 , GRCh37.p13 chr15: 40,414,149-64,343,006 , EIF4EBP2P2, 475 more genes
    nsv5005327copy number variation1nstd200human GRCh38 chr15: 43,352,096-43,393,954 , GRCh37.p13 chr15: 43,644,294-43,686,152 TUBGCP4, RN7SL487P, 2 more genes
    nsv5005326copy number variation1nstd200human GRCh38 chr15: 43,351,993-43,352,159 , GRCh37.p13 chr15: 43,644,191-43,644,357 ADAL
    nsv4872280inversion1nstd200human GRCh37 chr15: 40,414,149-64,343,008 , GRCh38.p12 chr15: 40,121,948-64,050,809 , DNAAF4-CCPG1, 475 more genes
    nsv4863762copy number variation1nstd200human GRCh37 chr15: 43,644,294-43,686,152 , GRCh38.p12 chr15: 43,352,096-43,393,954 TUBGCP4, ZSCAN29, 2 more genes
    nsv4729554copy number variation1nstd102humanLikely pathogenic GRCh37 chr15: 43,135,272-43,744,542 , GRCh38.p12 chr15: 42,843,074-43,452,344 EPB42, FDPSP4, 16 more genes
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